Clinical Research Site Director

ObjectiveHealth

$90K — $110K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • 5+ years of experience coordinating industry-sponsored clinical trials
  • Demonstrated leadership in site management
  • Proficient in patient interaction and care
  • Expertise in conducting IRB approved clinical trial protocols
  • Strong attention to detail for data and regulatory compliance
  • Effective communication with diverse stakeholders
  • Ability to handle multiple protocols and maintain focus

Responsibilities

  • Oversee and manage all aspects of assigned clinical trials
  • Ensure patient recruitment through screening and enrollment processes
  • Conduct clinic visits and perform direct patient care activities
  • Maintain compliance with protocols and regulatory bodies
  • Facilitate communication between research teams and external partners
  • Utilize provided technologies to optimize daily operations
  • Support a culture of continuous improvement and adherence to core values

Benefits

  • 401(k) plan with company match
  • Clear career advancement pathways
  • Short- and long-term disability insurance
  • Health, dental, and vision insurance options
  • Generous paid time off policy
  • Paid holidays and adoption assistance
  • Flexible spending and health savings accounts
Full Job Description
Clinical Research Site Director

ObjectiveHealth is currently seeking a qualified candidate for the full-time position of Clinical Research Site Director. The ideal candidate will have prior experience in site leadership and 5 years of experience coordinating industry-sponsored clinical trials.

Who You Are
  • A lover of patient interaction and skilled at providing patient care
  • A team player with a bias for action and an attitude that takes personal responsibility
  • A proven leader among your peers and teams
  • Skilled in all aspects required for conducting an IRB approved clinical trial protocol: identification, screening, randomization, and enrollment of patients, conducting clinic visits, etc.
  • Skilled at performing and assisting with direct patient care activities: consenting patients, physical assessments, blood draws, medication administration, ECG, etc.
  • Possess an acute attention to detail for clean data entry, regulatory compliance, productive site visits, efficient study set-up and maintenance, and strict protocol adherence
  • An expert communicator with the goal of fostering relationships between the research team, PIs, Sponsors, Monitors, and others
  • A strong advocate for Company values, mission, and initiatives
  • Not easily distracted: You have the ability to stay focused while running different protocols, resolving and submitting IRB responses and audit findings, tracking AE and SAE events, and maintaining eSource material for assigned studies
  • Energized by the idea of playing a role in the future of new therapy development in the areas of Gastroenterology, Urology, Respiratory, Orthopedics, Dermatology, and/or Oncology


What Success Looks Like for This Role
  • Taking ownership of assigned studies and patients
  • Communicating promptly and effectively with leadership and coworkers when you have a question or see something that needs correction
  • Showing up on time, every time
  • Ensuring strict compliance to the laws, regulations, and requirements of all applicable governing bodies
  • Learning and using the technologies we provide to enhance your day-to-day activities
  • Embodying our core values of Compassion, Integrity, Collaboration, Innovation, Velocity, and Dedication


What We Offer

Competitive compensation, 401(k) with Company match, a clear career pathway for advancement within the Company, Short- and Long-Term Disability, Health Savings and Flexible Spending Accounts, Health, Dental and Vision insurance Plans, Generous PTO, Adoption Assistance, Paid Holidays, and a wide selection of other voluntary benefits.

Requirements

This job requires legal authorization to work in the US. We are not currently accepting work visas.

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